Clinical Research Associate

**About CERC**

We at The European Center for Cardiovascular Research (CERC) are a CRO specialized in the design and management of international clinical trials dedicated to cardiovascular diseases.

Chaired by 5 interventional cardiologists, who have been key clinical research investigators for over 20 years, we conduct clinical studies directly in line with the issues of cardiologists practicing in private or public hospitals.

CERC is currently managing thirty studies sponsored by the industry, as well as more than 10 “investigator-initiated trials” set up to find treatments for conditions / comorbidities for which no satisfactory therapeutic strategies have yet been developed.

The **Clinical Research Associate **is responsible for the monitoring of clinical trials and tracking study progress.

You will work closely with a CERC Project Leader. And make valuable contributions to the development of innovative techniques, concepts, and treatments to improve patient care and lives.

We are looking for a **Spanish and english** speaking **Clinical Research Associate**. If you speak French too it would be a huge advantage.

Additional languages are welcome.

**We’re looking for an enthusiastic team player who will focus on**:

- Site management from initiation to close-out in accordance with study specific procedures, applicable SOPs, and ICH GCP guidelines
- Remote monitoring via e-CRF
- Training and information for investigators and the clinical study
- Privileged contact with investigators centers
- On site monitoring of patient safety (review of SAEs, AEs)
- Drafting of visit reports in compliance with the monitoring plan
- Updating of all relevant tracking systems on an ongoing basis
- Assisting the Clinical Project Leader in regulatory submissions and site contract management when necessary.

**You will be successful in this role if**:

- You have an excellent interpersonal, verbal and written communication skills
- You have the ability to prioritize multiple tasks and achieve project timelines
- You have the ability to take initiative and work autonomously
- You have computer skills (Microsoft Office)
- You have a Master or higher graduate degree within a science related field, with a CRA training certificate
- You have experience in performing a Clinical Research Associate role

**What’s in it for you?**
- Flexible working hours
- Multicultural environment
- Eco-friendly company
- Regular in-house training sessions

At CERC, you will be part of a close-knit organisation, you will have the opportunity to learn and interact directly with different teams (regulatory affairs department, data managers, core lab specialists, finance manager, etc ). We have a friendly and open collaborative culture and a united team vision.

You will help in the creation of new innovative solutions to improve patient care.

**Working With CERC**
Open position is immediately available.
The salary range is depending on seniority.
Position is based in Massy, France.
Please send us your CV and Cover Letter in english.

Type d'emploi : CDI
Statut : Cadre

Rémunération : 41 000,00€ à 46 000,00€ par an

Avantages:

- RTT

Programmation:

- Du lundi au vendredi
- Flextime
- Travail en journée

Question(s) de présélection:

- Quelle est votre disponibilité pour une prise de poste ?

Langue:

- Spanish (Requis)

Lieu du poste : En présentiel